Differentiation of human embryonic stem cells on three-dimensional polymer scaffolds

dc.contributor.authorLevenberg, Shulamit
dc.contributor.authorHuang, Ngan F.
dc.contributor.authorLavik, Erin
dc.contributor.authorRogers, Arlin B.
dc.contributor.authorItskovitz-Eldor, Joseph
dc.contributor.authorLanger, Robert
dc.date.accessioned2021-03-19T17:12:33Z
dc.date.available2021-03-19T17:12:33Z
dc.date.issued2003-10-28
dc.descriptionProceedings of the National Academy of Sciences Oct 2003, 100 (22) 12741-12746en_US
dc.description.abstractHuman embryonic stem (hES) cells hold promise as an unlimited source of cells for transplantation therapies. However, control of their proliferation and differentiation into complex, viable 3D tissues is challenging. Here we examine the use of biodegradable polymer scaffolds for promoting hES cell growth and differentiation and formation of 3D structures. We show that complex structures with features of various committed embryonic tissues can be generated, in vitro, by using early differentiating hES cells and further inducing their differentiation in a supportive 3D environment such as poly(lactic-co-glycolic acid)/poly(L-lactic acid) polymer scaffolds. We found that hES cell differentiation and organization can be influenced by the scaffold and directed by growth factors such as retinoic acid, transforming growth factor β, activin-A, or insulin-like growth factor. These growth factors induced differentiation into 3D structures with characteristics of developing neural tissues, cartilage, or liver, respectively. In addition, formation of a 3D vessel-like network was observed. When transplanted into severe combined immunodeficient mice, the constructs continue to express specific human proteins in defined differentiated structures and appear to recruit and anastamose with the host vasculature. This approach provides a unique culture system for addressing questions in cell and developmental biology, and provides a potential mechanism for creating viable human tissue structures for therapeutic applications.en_US
dc.description.sponsorshipWe thank Ernest Smith, Kathleen Cormier and Jeff Bajko for excellent assistance in tissue embedding and processing, Robert Marini for help with animal procedures, Mara Macdonald and Susan Matthews for help with staining and data analysis, and Justin S. Golub for help with RT-PCR assays. We also thank Keith Ligon for his advice and assistance with histology assessment. This work was supported by National Institutes of Health Grant HL60435.en_US
dc.description.urihttps://www.pnas.org/content/100/22/12741.shorten_US
dc.format.extent6 pagesen_US
dc.genreconference papers and proceedingsen_US
dc.identifierdoi:10.13016/m2fdtt-iqqx
dc.identifier.citationShulamit Levenberg, Ngan F. Huang, Erin Lavik, Arlin B. Rogers, Joseph Itskovitz-Eldor, Robert Langer, Differentiation of human embryonic stem cells on three-dimensional polymer scaffolds, Proceedings of the National Academy of Sciences Oct 2003, 100 (22) 12741-12746; DOI: 10.1073/pnas.1735463100en_US
dc.identifier.urihttps://doi.org/10.1073/pnas.1735463100
dc.identifier.urihttp://hdl.handle.net/11603/21194
dc.language.isoen_USen_US
dc.publisherPNASen_US
dc.relation.isAvailableAtThe University of Maryland, Baltimore County (UMBC)
dc.relation.ispartofUMBC Chemical, Biochemical & Environmental Engineering Department Collection
dc.rightsThis item is likely protected under Title 17 of the U.S. Copyright Law. Unless on a Creative Commons license, for uses protected by Copyright Law, contact the copyright holder or the author.
dc.subjecthuman embryonic stem (hES)en_US
dc.subjecttransplantationen_US
dc.subject3D tissuesen_US
dc.subjectretinoic aciden_US
dc.titleDifferentiation of human embryonic stem cells on three-dimensional polymer scaffoldsen_US
dc.typeTexten_US

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